ABACUSRecalls & reported problems across all models

We found 3 models of ABACUS by Baxter Healthcare Corporation in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

1 FDA recall record name at least one of these models by its device identifier.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

ABACUS recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Jun 22, 2022Terminated

   There is a potential risk of medication error when using specific Abacus Order Entry & Calculation software.

   Z-1376-2022 · Root cause: Software design · names 3 of these models · Recall details · FDA record ↗

ABACUS models

3 models, most reported first. Each model has its own page with its reports, recalls and device details.

• ABACUS 83003391

  SYSTEM/DEVICE, PHARMACY COMPOUNDING
  1 recall0 reports
• ABACUS 83003392

  SYSTEM/DEVICE, PHARMACY COMPOUNDING
  1 recall0 reports
• ABACUS 83003393

  SYSTEM/DEVICE, PHARMACY COMPOUNDING
  1 recall0 reports

Other Baxter Healthcare Corporation products

• EXACTAMIX28 models · 6,739 reports · 13 recalls
• MiniCap3 models · 3,423 reports · 7 recalls
• Novum IQ3 models · 1,540 reports · 7 recalls
• CLEARLINK/CONTINU-FLO/DUO-VENT3 models · 873 reports · 3 recalls
• CLEARLINK19 models · 710 reports · 4 recalls
• CLEARLINK/CONTINU-FLO8 models · 416 reports · 4 recalls
• CLEARLINK/DUO-VENT5 models · 282 reports · 1 recall
• REPEATER6 models · 189 reports